Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance.
- NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_assertion description "[Microarray-based comparative genomic hybridization (array-CGH) is considered to be superior for the investigation of chromosomal aberrations in children with MR, and has been demonstrated to improve the diagnostic detection rate of these small chromosomal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance.
- NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_assertion evidence source_evidence_literature NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance.
- NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_assertion SIO_000772 17901693 NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance.
- NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_assertion wasDerivedFrom befree-2016 NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance.
- NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_assertion wasGeneratedBy ECO_0000203 NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance.
- befree-2016 importedOn "2016-02-19" NP632349.RA7Ph8jT9LUL8MdPzVK5VWn0iK6hzlVZjkIGDtkZi2BzY130_provenance.